Development IGF-1 receptor signaling

Pathway network for the Development IGF-1 receptor signaling SuperPath

Sources:
  • GeneGo (Thomson Reuters)

Gene overlap in member pathways for Development IGF-1 receptor signaling SuperPath

Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways

Disorders associated with Development IGF-1 receptor signaling SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1HemimegalencephalyEnrichmentAKT3, MTOR, PIK3CA, PTEN, RHEB11.23
2Focal cortical dysplasia, type iiEnrichmentMTOR, RHEB, TSC1, TSC29.49
3Isolated focal cortical dysplasia type iiEnrichmentMTOR, RHEB, TSC1, TSC29.49
4Noonan syndrome 1EnrichmentHRAS, MAP2K1, MAP2K2, RAF1, SOS1, SOS29.20
5RasopathyEnrichmentHRAS, MAP2K1, MAP2K2, RAF1, SOS1, SOS28.87
6Noonan syndrome and noonan-related syndromeEnrichmentHRAS, MAP2K1, MAP2K2, RAF1, SOS18.35
7Adult hepatocellular carcinomaEnrichmentPIK3CA, TP53, TSC1, TSC27.46
8Colorectal cancerEnrichmentAKT1, BAX, CCND1, MET, PIK3CA, PIK3R1, TP537.15
9Bladder cancerEnrichmentCDKN1A, PIK3CA, PTEN, TP53, TSC16.92
10Ovarian cancerEnrichmentAKT1, CDKN1B, MET, PIK3CA, PTEN, TP53, TSC26.70
11Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentAKT3, PIK3CA, PIK3R26.55
12Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1EnrichmentAKT3, CCND2, PIK3R26.55
13Breast adenocarcinomaEnrichmentAKT1, PIK3CA, TP535.86
14Noonan syndrome 3EnrichmentHRAS, RAF1, SOS15.52
15Cowden syndromeEnrichmentAKT1, PIK3CA, PTEN5.24
16Arteriovenous malformationEnrichmentHRAS, MAP2K1, PIK3CA5.15
17Myopathy, x-linked, with excessive autophagyEnrichmentHRAS, MAP2K1, PIK3CA4.99
18Lung non-small cell carcinomaEnrichmentHRAS, MAP2K1, PIK3CA4.86
19MeningiomaEnrichmentAKT1, PIK3CA, PTEN4.82
20LymphangioleiomyomatosisEnrichmentTSC1, TSC24.76
21Inherited cancer-predisposing syndromeEnrichmentCDKN1B, MET, PTEN, TP53, TSC1, TSC24.74
22Immunoglobulin kappa light chain deficiencyEnrichmentIGK, IGKC4.70
23Hereditary breast carcinomaEnrichmentAKT1, PIK3CA, PTEN, TP534.47
24Tuberous sclerosis 1EnrichmentTSC1, TSC24.28
25Nasopharyngeal carcinomaEnrichmentNFKBIA, TP534.28
26Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentPIK3CA, PIK3R14.28
27Immunodeficiency 14a with lymphoproliferation, autosomal dominantEnrichmentPIK3CD, PIK3R14.28
28HamartomaEnrichmentTSC1, TSC24.28
29Immunodeficiency 14EnrichmentPIK3CD, PIK3R14.28
30Recurrent infections associated with rare immunoglobulin isotypes deficiencyEnrichmentIGK, IGKC4.23
31Hepatocellular carcinomaEnrichmentMET, PIK3CA, TP533.99
32Tuberous sclerosisEnrichmentTSC1, TSC23.98
33Cardiofaciocutaneous syndrome 1EnrichmentMAP2K1, MAP2K23.93
34Cardiofaciocutaneous syndromeEnrichmentMAP2K1, MAP2K23.93
35Acute megakaryocytic leukemiaEnrichmentPTEN, TP533.76
36Prostate cancerEnrichmentPIK3CA, PTEN, TP533.62
37Insulin-like growth factor iEnrichmentIGF1, IGF1R3.60
38Li-fraumeni syndromeEnrichmentMDM2, TP533.59
39Cowden syndrome 1EnrichmentPIK3CA, PTEN3.59
40Breast cancerEnrichmentAKT1, PIK3CA, PTEN, TP533.56
41Lung cancerEnrichmentFASLG, MET, PIK3CA3.49
42Multiple endocrine neoplasia, type iEnrichmentCDKN1A, CDKN1B3.44
43Squamous cell carcinoma, head and neckEnrichmentPTEN, TP533.44
44Renal cell carcinoma, papillary, 1EnrichmentMET, MTOR3.44
45Gallbladder cancerEnrichmentPIK3CA, TP533.44
46Common variable immunodeficiencyEnrichmentNFKB1, NFKB23.44
47Overgrowth syndromeEnrichmentMTOR, PIK3R13.44
48Hemihyperplasia, isolatedEnrichmentIGF2, PIK3CA3.42
49Nevus, epidermalEnrichmentHRAS, PIK3CA3.39
50Capillary malformation-arteriovenous malformation 1EnrichmentMAP2K1, PIK3CA3.39
51Thyroid cancer, nonmedullary, 2EnrichmentHRAS, PTEN3.28
52Follicular thyroid carcinomaEnrichmentHRAS, PTEN3.28
53Melanocytic nevus syndrome, congenitalEnrichmentHRAS, RAF13.26
54Leukemia, chronic lymphocyticEnrichmentCCND1, TP533.12
55Autosomal non-syndromic agammaglobulinemiaEnrichmentPIK3CD, PIK3R13.12
56Gastric cancerEnrichmentPIK3CA, PTEN, TP533.11
57Type 2 diabetes mellitusEnrichmentAKT2, IRS1, IRS23.06
58Lip and oral cavity carcinomaEnrichmentPIK3CA, TP532.95
59Nk-cell enteropathyEnrichmentIGF1R, PIK3CB2.88
60Specific learning disabilityEnrichmentMAPK1, RPS6KA32.87
61Myeloma, multipleEnrichmentCCND1, PIK3R2, TP532.78
62Renal cell carcinoma, nonpapillaryEnrichmentMET, MTOR2.75
63RhabdomyosarcomaEnrichmentPTEN, TP532.70
64GliosarcomaEnrichmentNFKBIA, TP532.70
65Giant cell glioblastomaEnrichmentNFKBIA, TP532.64
66Diffuse large b-cell lymphomaEnrichmentPTEN, TP532.55
67Endometrial cancerEnrichmentPIK3CA, PTEN2.46
68MacrodactylyEnrichmentPIK3CA2.38
69Proteus syndromeEnrichmentAKT12.38
70Hypoinsulinemic hypoglycemia with hemihypertrophyEnrichmentAKT22.38
71Vacterl association with hydrocephalusEnrichmentPTEN2.38
72Deafness, autosomal recessive 26EnrichmentGAB12.38
73Megalencephaly, autosomal dominantEnrichmentPIK3CA2.38
74Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3EnrichmentCCND22.38
75Cowden syndrome 5EnrichmentPIK3CA2.38
76Fetal encasement syndromeEnrichmentCHUK2.38
77Accelerated tumor formationEnrichmentMDM22.38
78Cerebral cavernous malformations 4EnrichmentPIK3CA2.38
79Immunodeficiency 15bEnrichmentIKBKB2.38
80Immunodeficiency 15aEnrichmentIKBKB2.38
81Immunodeficiency 92EnrichmentREL2.38
82Lessel-kubisch syndromeEnrichmentMDM22.38
83Short syndromeEnrichmentPIK3R12.38
84Bone marrow failure syndrome 5EnrichmentTP532.38
85Osteofibrous dysplasiaEnrichmentMET2.38
86Papilloma of choroid plexusEnrichmentTP532.38
87Basal cell carcinoma 7EnrichmentTP532.38
88Anaplastic thyroid carcinomaEnrichmentTP532.38
89Papillary tumor of the pineal regionEnrichmentPTEN2.38
90Deafness, autosomal recessive 97EnrichmentMET2.38
91Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2EnrichmentAKT32.38
92Hemifacial myohyperplasiaEnrichmentPIK3CA2.38
93Capillary malformation of the lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowthEnrichmentPIK3CA2.38
94Neuroendocrine tumorEnrichmentCDKN1B2.38
95Autism 9EnrichmentMET2.38
96Immunodeficiency 36 with lymphoproliferationEnrichmentPIK3R12.38
97Cowden syndrome 6EnrichmentAKT12.38
98Immunodeficiency 14b, autosomal recessiveEnrichmentPIK3CD2.38
99Ataxia-telangiectasia-like disorder 2EnrichmentPCNA2.38
100Agammaglobulinemia 7, autosomal recessiveEnrichmentPIK3R12.38
101Glioma susceptibility 2EnrichmentPTEN2.38
102Ductal carcinoma in situEnrichmentTP532.38
103Deficiency in anterior pituitary function - variable immunodeficiency syndromeEnrichmentNFKB22.38
104Immunodeficiency 53EnrichmentRELB2.38
105Bartsocas-papas syndrome 2EnrichmentCHUK2.38
106Segmental progressive overgrowth syndrome with fibroadipose hyperplasiaEnrichmentPIK3CA2.38
107Thyroid gland undifferentiated carcinomaEnrichmentTP532.38
108Small-cell carcinoma of the ovary of hypercalcemic typeEnrichmentTP532.38
109Arthrogryposis, distal, type 11EnrichmentMET2.38
110HypospadiasEnrichmentPIK3CA2.38
111Capillary hemangiomaEnrichmentAKT32.38
112Diffuse pediatric-type high-grade glioma, h3-wildtype and idh-wildtypeEnrichmentTP532.38
113Choroid plexus cancerEnrichmentTP532.38
114Rare venous malformationEnrichmentPIK3CA2.38
115Diaphragmatic eventrationEnrichmentPIK3CA2.38
116Pik3ca-related overgrowth spectrumEnrichmentPIK3CA2.38
117Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to ikbka deficiencyEnrichmentCHUK2.38
118Pleomorphic xanthoastrocytomaEnrichmentTP532.38
119Rare combined vascular malformationEnrichmentPIK3CA2.38
120Cavernous lymphangiomaEnrichmentPIK3CA2.38
121Pik3ca-related overgrowth syndromeEnrichmentPIK3CA2.38
122Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndromeEnrichmentPTEN2.38
123Hemihyperplasia-multiple lipomatosis syndromeEnrichmentPIK3CA2.38
124Eccrine angiomatous hamartomaEnrichmentPIK3CA2.38
125Macrodactyly of toeEnrichmentPIK3CA2.38
126Akt2-related familial partial lipodystrophyEnrichmentAKT22.38
127Noonan syndrome 5EnrichmentRAF12.35
128Noonan syndrome 4EnrichmentSOS12.35
129Melorheostosis, isolatedEnrichmentMAP2K12.35
130Cardiomyopathy, dilated, 1nnEnrichmentRAF12.35
131Cardiofaciocutaneous syndrome 3EnrichmentMAP2K12.35
132Noonan syndrome 9EnrichmentSOS22.35
133Noonan syndrome 13EnrichmentMAPK12.35
134Hyper-ige syndrome 6, autosomal dominant, with recurrent infectionsEnrichmentSTAT62.35
135MelorheostosisEnrichmentMAP2K12.35
136Leopard syndrome 2EnrichmentRAF12.35
137Cardiofaciocutaneous syndrome 4EnrichmentMAP2K22.35
138TrigonitisEnrichmentRAF12.35
139T-b+ severe combined immunodeficiency due to jak3 deficiencyEnrichmentJAK32.35
140B-lymphoblastic leukemia/lymphoma with t(5;14)(q31.1;q32.3)EnrichmentIGH2.35
141Phakomatosis pigmentokeratoticaEnrichmentHRAS2.35
142Mendelian susceptibility to mycobacterial diseases due to partial jak1 deficiencyEnrichmentJAK12.35
143Coffin-lowry syndromeEnrichmentRPS6KA32.29
144Intellectual developmental disorder, x-linked 19EnrichmentRPS6KA32.29
145Symptomatic form of coffin-lowry syndrome in female carriersEnrichmentRPS6KA32.29
146Distal 17p13.3 microdeletion syndromeEnrichmentYWHAE2.29
147Burkitt lymphomaEnrichmentMYC2.08
148Adrenocortical carcinoma, hereditaryEnrichmentTP532.08
149Cervical cancerEnrichmentTP532.08
150Ectodermal dysplasia and immunodeficiency 2EnrichmentNFKBIA2.08
151Keratosis, seborrheicEnrichmentPIK3CA2.08
152Roifman-chitayat syndromeEnrichmentPIK3CD2.08
153Noonan syndrome 8EnrichmentPIK3CA2.08
154Lymphoma, hodgkin, classicEnrichmentTP532.08
155Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.08
156Immunodeficiency, common variable, 10EnrichmentNFKB22.08
157Multiple endocrine neoplasia, type ivEnrichmentCDKN1B2.08
158Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA2.08
159Cebalid syndromeEnrichmentMTOR2.08
160Childhood hepatocellular carcinomaEnrichmentMET2.08
161Rela fusion-positive ependymomaEnrichmentRELA2.08
162Glycogen storage disease 0, muscleEnrichmentGYS12.08
163Senior-loken syndrome 7EnrichmentAKT32.08
164Rosette-forming glioneuronal tumorEnrichmentPIK3CA2.08
165Papillary renal cell carcinomaEnrichmentMET2.08
166Congenital fibrosarcomaEnrichmentTP532.08
167Li-fraumeni syndrome 1EnrichmentTP532.08
168SarcomaEnrichmentTP532.08
169Ectodermal dysplasia and immune deficiencyEnrichmentNFKBIA2.08
170Cervix carcinomaEnrichmentTP532.08
171Immune system diseaseEnrichmentPIK3CD2.08
172Hodgkin's lymphomaEnrichmentTP532.08
173Bardet-biedl syndrome 16EnrichmentAKT32.08
174Smith-kingsmore syndromeEnrichmentMTOR2.08
175Houge-janssens syndrome 3EnrichmentPPP2CA2.08
176Vacterl with hydrocephalusEnrichmentPTEN2.08
177Glycogen storage disease due to muscle and heart glycogen synthase deficiencyEnrichmentGYS12.08
178Common variable immunodeficiency 12EnrichmentNFKB12.08
179Juvenile polyposis of infancyEnrichmentPTEN2.08
180Pleomorphic rhabdomyosarcomaEnrichmentTP532.08
181Hypoparathyroidism, sensorineural deafness, and renal dysplasia syndromeEnrichmentGATA32.05
182Fibromatosis, gingival, 1EnrichmentSOS12.05
183Costello syndromeEnrichmentHRAS2.05
184Hemangiopericytoma, malignantEnrichmentSTAT62.05
185Pulmonic stenosisEnrichmentSOS12.05
186Autoinflammation, immune dysregulation, and eosinophiliaEnrichmentJAK12.05
187B-lymphoblastic leukemia/lymphoma with hyperdiploidyEnrichmentGATA32.05
188Hypoparathyroidism-deafness-renal disease syndromeEnrichmentGATA32.05
189Autosomal dominant nonsyndromic deafnessEnrichmentGATA32.05
190Tafro syndromeEnrichmentMAP2K22.05
191Wooly hair nevusEnrichmentHRAS2.05
192Severe combined immunodeficiencyEnrichmentIKBKB, JAK32.02
193Histiocytoma, angiomatoid fibrousEnrichmentCREB11.99
194Silver-russell syndrome 3EnrichmentIGF21.99
195Growth delay due to insulin-like growth factor type 1 deficiencyEnrichmentIGF11.99
196Silver-russell syndrome due to an imprinting defect of 11p15EnrichmentIGF21.99
197Silver-russell syndrome due to 11p15 microduplicationEnrichmentIGF21.99
198Pompe disease, infantile-onsetEnrichmentPIK3CA1.90
199Immunodeficiency 98 with autoinflammation, x-linkedEnrichmentFASLG1.90
200Polycystic kidney disease, infantile severe, with tuberous sclerosisEnrichmentTSC21.90
201Osteogenic sarcomaEnrichmentTP531.90
202Tuberous sclerosis 2EnrichmentTSC21.90
203High-grade b-cell lymphoma double-hit/triple-hitEnrichmentMYC1.90
204Dedifferentiated liposarcomaEnrichmentMDM21.90
205Atypical teratoid rhabdoid tumorEnrichmentTP531.90
206Anaplastic astrocytomaEnrichmentTP531.90
207Xanthinuria, type iiEnrichmentTSC21.90
208Squamous cell carcinomaEnrichmentTP531.90
209T-cell acute lymphoblastic leukemiaEnrichmentBAX1.90
210AdenocarcinomaEnrichmentTP531.90
211Laryngeal squamous cell carcinomaEnrichmentPTEN1.90
212Bone osteosarcomaEnrichmentTP531.90
213Growth delay due to insulin-like growth factor i resistanceEnrichmentIGF1R1.90
214Well-differentiated liposarcomaEnrichmentMDM21.90
215Renal cell carcinomaEnrichmentMET1.90
216KeratoacanthomaEnrichmentPIK3CA1.90
217Systemic lupus erythematosusEnrichmentIGHG1, SOCS11.88
218Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiencyEnrichmentJAK31.87
219Immune thrombocytopeniaEnrichmentSOCS11.87
220Severe combined immunodeficiency, x-linkedEnrichmentIL2RG1.87
221Agammaglobulinemia 1, autosomal recessiveEnrichmentIGH1.87
222Nuchal bleb, familialEnrichmentSOS11.87
223Langerhans cell histiocytosisEnrichmentMAP2K11.87
224Combined immunodeficiency, x-linkedEnrichmentIL2RG1.87
225Autoinflammatory syndrome, familial, with or without immunodeficiencyEnrichmentSOCS11.87
226Agammaglobulinemia 1EnrichmentIGH1.87
227Large congenital melanocytic nevusEnrichmentHRAS1.87
228Breast implant-associated anaplastic large cell lymphomaEnrichmentJAK11.87
229End stage renal diseaseEnrichmentGATA31.87
230SpermatocytomaEnrichmentHRAS1.87
231Miller-dieker lissencephaly syndromeEnrichmentYWHAE1.82
232Chromosome 17p13.3, centromeric, duplication syndromeEnrichmentYWHAE1.82
233Melanoma of soft tissueEnrichmentCREB11.82
234Beckwith-wiedemann syndrome due to imprinting defect of 11p15EnrichmentIGF21.82
235Small cell cancer of the lungEnrichmentTP531.78
236Thyroid cancer, nonmedullary, 1EnrichmentTP531.78
237Autoimmune lymphoproliferative syndromeEnrichmentFASLG1.78
238Immunodeficiency, common variable, 1EnrichmentNFKB21.78
239Mantle cell lymphomaEnrichmentCCND11.78
240Lung sarcomatoid carcinomaEnrichmentTP531.78
241Cerebrovascular diseaseEnrichmentPIK3CA1.78
242Embryonal rhabdomyosarcomaEnrichmentTP531.78
243Familial cerebral cavernous malformationsEnrichmentPIK3CA1.78
244Primary hyperparathyroidismEnrichmentCDKN1B1.78
245GliomaEnrichmentPTEN1.78
246Schimmelpenning-feuerstein-mims syndromeEnrichmentHRAS1.75
247Anemia, autoimmune hemolyticEnrichmentSOCS11.75
248Neurofibromatosis-noonan syndromeEnrichmentMAP2K21.75
249Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK11.75
250Noonan syndrome with multiple lentiginesEnrichmentRAF11.75
251Epidermolytic nevusEnrichmentHRAS1.75
252Adenosine deaminase deficiencyEnrichmentJAK31.75
253Gingival fibromatosisEnrichmentSOS11.75
254Male infertility due to gonadal dysgenesis or sperm disorderEnrichmentSOS21.75
255Autism spectrum disorderEnrichmentMAP2K1, PTEN, TSC21.74
256Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentYWHAZ1.69
257Silver-russell syndrome due to a point mutationEnrichmentIGF21.69
258Capillary malformations, congenitalEnrichmentPIK3CA1.68
259Von hippel-lindau syndromeEnrichmentCCND11.68
260Rhabdomyosarcoma 2EnrichmentTP531.68
261Macrocephaly/autism syndromeEnrichmentPTEN1.68
262LymphomaEnrichmentTP531.68
263HemangiomaEnrichmentPTEN1.68
264Lymphoma, mucosa-associated lymphoid typeEnrichmentIGH1.65
265Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-negativeEnrichmentJAK31.65
266Follicular lymphomaEnrichmentIGH1.65
267Hereditary breast ovarian cancer syndromeEnrichmentPTEN, TP531.65
268Klippel-trenaunay-weber syndromeEnrichmentPIK3CA1.60
269Congenital anomalies of kidney and urinary tract 1EnrichmentTRAP11.60
270KeratoconusEnrichmentTSC11.60
271Adrenocortical carcinomaEnrichmentTP531.60
272Lung squamous cell carcinomaEnrichmentPIK3CA1.60
273Endometrial stromal sarcomaEnrichmentYWHAE1.60
274HypertelorismEnrichmentPIK3CA, RPS6KA31.54
275Esophageal cancerEnrichmentTP531.54
276Polycystic kidney disease 1 with or without polycystic liver diseaseEnrichmentTSC21.54
277Polycystic kidney disease 1EnrichmentTSC21.54
278Essential thrombocythemiaEnrichmentTP531.54
279MegacolonEnrichmentAKT31.54
280B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)EnrichmentTP531.54
281Kidney clear cell sarcomaEnrichmentYWHAE1.52
282Pilomyxoid astrocytomaEnrichmentRAF11.51
283Arthrogryposis, distal, type 1aEnrichmentMET1.48
284Glioma susceptibility 1EnrichmentTP531.48
285Lymphoma, non-hodgkin, familialEnrichmentTP531.48
286Silver-russell syndrome 1EnrichmentIGF21.45
287Primary hyperaldosteronismEnrichmentTP531.43
288Gastroesophageal refluxEnrichmentRPS6KA31.40
289Orthostatic intoleranceEnrichmentRPS6KA31.40
290Ciliary dyskinesia, primary, 3EnrichmentNFKB11.38
291PolymicrogyriaEnrichmentAKT31.38
292MelanomaEnrichmentPTEN1.38
293Familial colorectal cancerEnrichmentTP531.38
294Omenn syndromeEnrichmentIL2RG1.36
295Ventricular septal defectEnrichmentRPS6KA31.35
296Meningioma, familialEnrichmentPTEN1.34
297Myelodysplastic syndromeEnrichmentTP531.34
298Glycogen storage diseaseEnrichmentGYS11.34
299Uterine corpus cancerEnrichmentPTEN1.34
300AsthmaEnrichmentCCL111.32
301Combined immunodeficiencyEnrichmentIL2RG1.32
302Combined t cell and b cell immunodeficiencyEnrichmentIL2RG1.32
303Combined t and b cell immunodeficiencyEnrichmentIL2RG1.32
304Aortic valve disease 1EnrichmentSOS11.24
305Lung cancer susceptibility 3EnrichmentTP531.24
30646,xy partial gonadal dysgenesisEnrichmentSOS11.21
307Lynch syndromeEnrichmentPIK3CA1.21
308Autosomal dominant polycystic kidney diseaseEnrichmentTSC21.21
309Kidney diseaseEnrichmentTSC11.21
310Rare genetic intellectual disabilityEnrichmentMTOR1.21
311Congenital nervous system abnormalityEnrichmentPTEN, TSC21.14
312Nervous system diseaseEnrichmentPTEN, TSC21.14
313Wilms tumor 1EnrichmentIGF21.13
314Heart, malformation ofEnrichmentMAPK11.11
315Human immunodeficiency virus type 1EnrichmentCCL111.11
316HepatoblastomaEnrichmentTP531.07
317Beckwith-wiedemann syndromeEnrichmentIGF21.06
318Diamond-blackfan anemia 1EnrichmentTP531.03
319Precursor t-cell acute lymphoblastic leukemiaEnrichmentMYC1.03
320Pancreatic cancerEnrichmentTP531.00
321Cardiomyopathy, familial hypertrophic, 1EnrichmentRAF10.99
322Hydrops fetalis, nonimmuneEnrichmentHRAS0.96
323Severe covid-19EnrichmentJAK30.91
324Differentiated thyroid carcinomaEnrichmentHRAS0.91
325MicrocephalyEnrichmentIGF1R, MAPK10.89
326Non-immune hydrops fetalisEnrichmentHRAS0.88
327CakutEnrichmentTRAP10.87
328Familial hypertrophic cardiomyopathyEnrichmentRAF10.86
329Diamond-blackfan anemiaEnrichmentTP530.85
330Left ventricular noncompactionEnrichmentRAF10.84
331Leukemia, acute myeloidEnrichmentTP530.81
332Non-syndromic x-linked intellectual disabilityEnrichmentRPS6KA30.77
333West syndromeEnrichmentTSC20.77
334Familial isolated dilated cardiomyopathyEnrichmentRAF10.67
335Autosomal dominant non-syndromic intellectual disabilityEnrichmentYWHAZ0.65
336Dilated cardiomyopathyEnrichmentRAF10.52
337Rare autosomal recessive non-syndromic sensorineural deafness type dfnbEnrichmentMET0.50
338Complex neurodevelopmental disorderEnrichmentPPP2CA0.39

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